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Thieno[2,3-d][1,3]dithiole-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67188-88-9

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67188-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67188-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,8 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67188-88:
(7*6)+(6*7)+(5*1)+(4*8)+(3*8)+(2*8)+(1*8)=169
169 % 10 = 9
So 67188-88-9 is a valid CAS Registry Number.

67188-88-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name thieno[2,3-d][1,3]dithiole-2-thione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67188-88-9 SDS

67188-88-9Downstream Products

67188-88-9Relevant academic research and scientific papers

Synthesis of thieno[2,3-d]-1,3-dithiol-2-thiones from thieno[2,3-d]-1,2,3- thiadiazoles: Matryoshka-type autoclave for high-temperature, high-pressure thermolysis microscale reactions

Jordis, Ulrich,Bhattacharya, Kaberi,Boamah, Philip Y.,Lee, Ving J.

, p. 145 - 154 (2007/10/03)

Thieno[2,3-d]-1,2,3-thiadiazoles (1) react with carbon disulfide in a "Matryoshka-type" double compartment autoclave [1] to yield thieno[2,3-d]-1,3-dithiol-2-thiones (2). With BH3/Me2S the cyclic trithiocarbonate (2d) is cleaved and the product characterized after methylation as 4b. Compounds 7a and 7b are prepared via the thieno[2,3-d]-1,3- dithiolium salts (6) followed by NaBH4-reduction.

Novel selenocycle-fused TTF-type of electron donors forming conducting molecular complexes: Bis(ethyleneseleno)tetrathiafulvalene (BES-TTF), diselenolotetrathiafulvalene (DS-TTF), and bis(ethyleneseleno)tetraselenafulvalene (BES-TSF)

Jigami, Tetsuya,Takimiya, Kazuo,Otsubo, Tetsuo,Aso, Yoshio

, p. 8865 - 8872 (2007/10/03)

The title selenocycle-fused tetrathiafulvalene derivatives (BES-TTF and DS-TTF) and tetraselenafulvalene derivative (BES-TSF) have been synthesized as novel electron donors, and their conducting molecular complexes have been studied. Although DS-TTF formed only semiconducting complexes, BES-TTF and BES-TSF gave metallic complexes with various electron acceptors, such as TCNQ, ClO4-, PF6-, and AsF6-. Among them, the TCNQ complex of BES-TSF showed an extraordinarily high room-temperature conductivity of 2700 ± 500 S cm-1, which is of the highest class for a molecular complex. The complexes of BES-TTF underwent a typical metal-to-insulator transition at low temperature, characteristic of one-dimensional organic metals. On the other hand, complexes of BES-TSF were less temperature-dependent and remained highly conducting, even down to cryogenic temperature. The different behaviors of the three donors are discussed on the basis of the crystal structures of their representative complexes as elucidated by X-ray crystallographic analyses.

Synthesis of Several Isomeric Tetrathiafulvalene ?-Electron Donors with Peripheral Sulfur Atoms. A Study of Their Radical Cations

Rovira, Concepcio,Veciana, Jaume,Santalo, Nuria,Tarres, Judit,Cirujeda, Joan,et al.

, p. 3307 - 3313 (2007/10/02)

An efficient synthesis of one new (10) and three previously reported (9, 11, and 12) ?-electron donors, which have one sulfur atom in each of the outer five-membered rings attached to the TTF system, is presented.The radical cations derived from 9-11 have

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